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实验性急性胰腺炎中过氧化物酶体增殖物激活受体的转化研究见解

Translational Insights Into Peroxisome Proliferator-Activated Receptors in Experimental Acute Pancreatitis.

作者信息

Huang Wei, Szatmary Peter, Wan Meihua, Bharucha Shameena, Awais Muhammad, Tang Wenfu, Criddle David N, Xia Qing, Sutton Robert

机构信息

From the *Department of Integrated Traditional and Western Medicine, Sichuan Provincial Pancreatitis Center, West China Hospital, Sichuan University, Chengdu, China; †NIHR Liverpool Pancreas Biomedical Research Unit, Royal Liverpool University Hospital; and ‡Department of Cellular and Molecular Physiology, University of Liverpool, Liverpool, United Kingdom.

出版信息

Pancreas. 2016 Feb;45(2):167-78. doi: 10.1097/MPA.0000000000000472.

Abstract

Acute pancreatitis (AP) is an inflammatory disorder of the exocrine pancreas frequently associated with metabolic causes, contributing factors, or consequences, including hypertriglyceridemia, obesity, and disorders of intermediary metabolism, respectively. To date, there is no specific therapy for this disease. Future optimal therapy should correct both inflammatory and metabolic components of the disease. Peroxisome proliferator-activated receptors (PPARs) are lipid-sensing nuclear receptors that control inflammatory and metabolic pathways via ligand-dependent and ligand-independent mechanisms. There are 3 known subtypes, PPAR-α, PPAR-β/δ, and PPAR-γ, which are differentially expressed in various tissues. The PPARs interact closely with other transcription factors such as nuclear factor κB and signal tranducers and activators of transcription that have pivotal roles in the pathobiology of AP. In this comprehensive review, we summarize the role of PPARs in AP, highlighting important in vitro and in vivo experimental findings. Finally, we propose future research directions as well as potential translational use of PPAR agonists in the treatment of AP.

摘要

急性胰腺炎(AP)是一种外分泌性胰腺的炎症性疾病,常与代谢原因、促成因素或后果相关,分别包括高甘油三酯血症、肥胖和中间代谢紊乱。迄今为止,尚无针对该疾病的特异性治疗方法。未来的最佳治疗应纠正该疾病的炎症和代谢成分。过氧化物酶体增殖物激活受体(PPARs)是脂质感应核受体,通过依赖配体和不依赖配体的机制控制炎症和代谢途径。已知有3种亚型,即PPAR-α、PPAR-β/δ和PPAR-γ,它们在各种组织中差异表达。PPARs与其他转录因子密切相互作用,如在AP病理生物学中起关键作用的核因子κB以及信号转导和转录激活因子。在这篇综述中,我们总结了PPARs在AP中的作用,突出了重要的体外和体内实验结果。最后,我们提出了未来的研究方向以及PPAR激动剂在AP治疗中的潜在转化应用。

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